We describe an aromatic alcohol dehydrogenase with properties indicati
ng a novel type of function in the defense response of plants to patho
gens, To obtain the enzyme free of contamination with possible isoform
s, a parsley (Petroselinum crispum) cDNA comprising the entire coding
region of the elicitor-responsive gene, ELl3, was expressed in Escheri
chia coli, In accord with large amino acid sequence similarities with
established cinnamyl and benzyl alcohol dehydrogenases from other plan
ts, the enzyme efficiently reduced various cinnamyl and benzyl aldehyd
es using NADPH as a cc-substrate, Highest substrate affinities were ob
served for cinnamaldehyde, 4-coumaraldehyde and coniferaldehyde, where
as sinapaldehyde, one of the most efficient substrates of several prev
iously analyzed cinnamyl alcohol dehydrogenases and a characteristic p
recursor molecule of angiosperm lignin, was not converted, A single fo
rm of ELl3 mRNA was strongly and rapidly induced in fungal elicitor-tr
eated parsley cells, These results, together with earlier findings tha
t the ELl3 gene is strongly activated both in elicitor-treated parsley
cells and at fungal infection sites in parsley leaves, but not in lig
nifying tissue, suggest a specific role of this enzyme in pathogen def
ense-related phenylpropanoid metabolism.